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OptiLIFT Applicator

by Pollogen Ltd

OptiLIFT Applicator (25002080) is a Class II device made by Pollogen Ltd, listed in FDA GUDID since 28 Oct 2025 (UDI-DI 07290019147640), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290019147640 UDI-DI Date28 Oct 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Radio-frequency skin surface treatment system applicator
Model / Ref / Catalog
OptiLIFT Applicator, 25002080
Primary DI / UDI-DI
07290019147640
FDA product code
GEI, NGX
GMDN term
Radio-frequency skin surface treatment system applicator
Device class
Class II
Regulation number
878.4400, 890.5850
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories).

Other devices from Pollogen Ltd

See all devices from Pollogen Ltd →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)